I posted this question in Dev- list so re-posting to correct list with some additional information.<div>I have paired end  sequencing files on which I would like to call SNPs compared to databases well check sequence variation among samples. I dont have access to any local galaxy instance. My question are-</div>
<div>1. Is there a way that I can upload these large files to galaxy and analyze them then delete?</div><div>2. Is there a work flow to call SNPs and analyze and annotate SNPS in Galaxy, If some one know about a work flow summarized  by some one in addition to  Galaxy list that will be bonus.</div>
<div><br></div><div>Thanks</div><div><br></div><div>Kanwar</div>